Devices for water treatment

ABSTRACT

A device for use in water comprising a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and a moss contained within the interior cavity in which the carrier completely encloses the moss.

This application is a continuation of U.S. Ser. No. 11/106,049, filed Apr. 14, 2005, which claims the benefit of provisional application Ser. No. 60/562,196, filed Apr. 14, 2004, the contents of each of which are hereby incorporated herein by reference.

FIELD OF THE INVENTION

This invention relates to devices for water treatment, and in particular relates to devices comprising sphagnum moss.

BACKGROUND OF THE INVENTION

There are many types of water treatment systems, such as filtration and cleaning systems for swimming pools and aquariums. Many of these systems filter the water to remove suspended matter and reduce the cloudy appearance of the water. Preventing bacterial growth in water and removing contaminants from water are significant industrial, as well as household, problems. For example, industrial effluent should be cleaned to remove toxic compounds as well as to remove bacteria before it is dumped into lakes and rivers. Containers of water such as swimming pools, hot tubs, aquariums and the like must be kept clean to prevent the water from becoming cloudy and/or the container walls from becoming slimy. The water may be treated by active means such as a filter to remove particles and bacteria, and it may also be treated by passive means whereby a biocide is placed in a container and floated in the water.

It is common to use chemical means to keep the water clean and reduce growth of bacteria and other microorganisms. Ultraviolet light, chlorination, bromination, treatment with ions of copper and silver as well as treatment with ozone can be used to treat and/or disinfect water. These are typical biocides, that is, substances or energies that destroy living organisms. Of course care must be taken with all these methods because of the possible toxicity or damage to the user. Chemicals require careful handling to avoid environmental contamination as well as contact with the user.

“Sphagnum moss” is a generic expression that designates a range of botanical species that co-exist in a sphagnous bog. It should be noted that “peat moss” refers generally to a decomposed or composted sphagnum moss. Sphagnum moss is commonly harvested for use in various products. The petals, and not the stems, of the moss preferably may be harvested. Typically large pieces of plant material (roots, twigs, etc.) are removed and the moss may be processed further after harvesting by forming an aqueous slurry to extract very fine particles. Water is removed from the slurry and the moss is dried. The moss may be compressed prior to packaging or shipment. Various additives may be used to alter the absorption characteristics or mechanical properties of the moss. Because sphagnum moss is readily available and relatively inexpensive, it has been used in a variety of products, primarily for the absorption of fluids.

There is substantial need in the art for products that inhibit the growth of microorganisms such as bacteria, yeast, and algae. It would be desirable to have a means to maintain the clarity of water in a swimming pool, whirlpool bath, aquarium, and the like, for long periods of time, without shutting a system down for cleaning. The most desirable system would require very little maintenance and would be relatively inexpensive.

SUMMARY OF THE INVENTION

The invention provides a device for use in water comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss.

The invention provides a method of inhibiting microorganism growth comprising placing in water susceptible to bacterial growth a device for inhibiting microorganism growth in water, the device comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss, and wherein the device comprises an amount of the moss effective to inhibit microorganism growth in the water.

The invention provides a kit comprising sterilized, non-decomposed moss and a device for use in water comprising a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity, wherein the interior cavity can completely enclose the moss.

The invention provides a method of inhibiting microorganism growth comprising placing in water susceptible to microorganism growth a device for inhibiting microorganism growth in water, the device comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss, wherein the device comprises an amount of the moss effective to inhibit microorganism growth in the water, and periodically shocking the water with an appropriate chemical agent.

The invention provides a method of treating water comprising placing in water a device comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss, and wherein the device comprises an amount of the moss effective to remove cations other than hydrogen ions from the water.

It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory and are intended to provide further explanation of the invention as claimed.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A illustrates a perspective view of one embodiment of the device of this invention. FIG. 1B illustrates a side view, and FIG. 1C illustrates a cross-sectional view along line C-C of FIG. 1B.

FIG. 2A illustrates a perspective view of another embodiment of the device of this invention and FIG. 2B shows a side view of the moss used within the device shown in FIG. 2A.

FIG. 3 illustrates a perspective view of another embodiment of the device of this invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

We have discovered species of sphagnum moss that can be used to treat water such as in a swimming pool, spa, aquarium, whirlpool, and the like. It is believed that particular species of moss are particularly effective at inhibiting and/or preventing the growth of bacteria and other microorganisms.

In this invention, “bacteriostatic” refers to a material that inhibits the growth of bacteria. In common lexicography, the term “antibacterial” generally refers to a bacterial growth inhibitor. Both terms should be distinguished from “bactericidal” which refers to materials that kill bacteria upon contact.

In this invention, “water treatment” refers to a process by which water is kept clean, clear, and pleasant smelling in swimming pools, aquariums, spas, and the like. Spas are also known as whirlpools or hot tubs. When the water is agitated, less foaming is observed. The moss is believed to inhibit growth of bacteria and other microorganisms and it also may absorb compounds and substances that decrease water clarity.

In this invention, sphagnum papillosum (S. papillosum) and/or sphagnum cristatum (S. cristatum) can be used in water treatment devices. In preferred embodiments, the moss is enclosed or encapsulated in a mesh material that prevents the moss from disintegrating in an aqueous environment. Thus the moss can be held in a desired place in a pool, hot tub, whirlpool bath, and the like. Preferred mesh materials include those comprising polymers such as nylon or polypropylene, with mesh sizes ranging from about 0.1 to 1 mm. Polymers are generally preferred because they are inexpensive and may be resistant to degradation.

Suitable for use in this invention are S. papillosum, which can be harvested from bogs in northern Minnesota, U.S.A., and S. cristatum, which is commercially available as a compressed bale from Sutton's Moss of Dobson, Westland, New Zealand. These species of moss can be used by themselves or together in the devices and systems of this invention. Typically and preferably the moss is cleaned to remove small particles, such as dirt, and larger debris, such as roots and leaves. Commercially available moss may be fumigated before it is packaged by a manufacturer in order to destroy seeds.

In a preferred embodiment, the moss is cut by mechanical means into a desired size and shape. The moss preferably is then sterilized by autoclaving, exposure to ethylene oxide, or by other means known to one of skill in the art. Sterilization destroys living organisms in the moss and thus avoids any problems of undesirable or foreign bacteria being introduced into the environment where a device of this invention is used. The moss is then ready for use in a water treatment system or other applications.

We have found that a convenient, easy, effective, and inexpensive way of treating water is to place a portion of S. papillosum or S. cristatum in a floatation device that permits water to flow around and through the moss. Another way to use it is to encapsulate it in mesh and weight the mesh so that the moss will remain in the water. Any suitable means that will maintain contact of the moss with water is suitable for use. This device is then placed in the swimming pool, whirlpool, hot tub, etc., where it can come into contact with the water. We have found that treatment is remarkably effective in preventing growth of microorganisms and in keeping the water clean, clear and free of odor and foam. This is all the more remarkable because this is a passive system when compared to a filtration system which forces water through the moss. Of course it is to be understood that active filtration could be done with the device of this invention to treat the water.

When used in swimming pools, hot tubs, and the like, the water treatment devices described herein are preferably used in conjunction with materials that kill microorganisms. This is because these environments may have large loads of microorganisms, particularly bacteria, introduced at various times. Accordingly, standard practice is to filter the water, flush water lines, and test the water as necessary. The pH can be adjusted by using commercially available solutions. The water treatment devices of this invention are most desirably used in conjunction with an oxidizer, such as potassium monopersulfate, referred to as “chlorine free shock”. Potassium monopersulfate is known to increase the efficiency of chlorine purification products, but we have found that it is also particularly effective when used with the sphagnum moss devices described above.

The sphagnum moss of this invention can be used in any composition, material, device, or method where the inhibition of bacteria is desirable. Uses include the inhibition of microorganism growth, the reduction and/or prevention of odors, water treatment, and control of mold and fungal growth; and control of fermentation. Such devices and materials include absorbent products, such as diaper liners, feminine hygiene products, bandages, and wound dressings. In such products, the moss can be enclosed between membranes of differing liquid transmission characteristics. That is, for example, one membrane may be permeable to fluid and another membrane may be permeable to vapor. The moss can be incorporated into polymers and used as face masks. The moss can be encapsulated in membranes and used in food preservation products such as packaging wraps and liners to absorb liquid and odors. The moss can be used in water treatment products to keep water clean in storage tanks, aquariums, swimming pools, whirlpool baths, spas, and the like, as well as in water filtration devices. The moss can be used for waste water and sewage treatment. The moss can be shaped into, for example, discs or pellets, and used to absorb water from grain and other food products. The moss also can be used for fermentation control (such as in liquids or grains). The moss can be used for the control of fungal or bacterial diseases in lawns and gardens. The moss can be used for mold control products such as in storage containers or ductwork linings.

The invention provides a device for use in water comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss. The carrier can comprise a float. The carrier can comprise a float and a cylindrical portion beneath the float, the cylindrical portion having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity. The moss can be enclosed within a mesh bag. The carrier can comprise one or more weights.

The moss can be non-decomposed moss. The moss can be sphagnum moss. The moss can be selected from the group consisting of sphagnum papillosum, sphagnum cristatum, and mixtures thereof. The moss can be compressed and can be in the form of strips. The moss can be sterilized by autoclaving, sterilized by chemical treatment, or sterilized by treatment with ethylene oxide. The moss can be washed with an acidic solution, especially a solution of acetic acid. The moss can be washed with an acidic solution and then washed with a salt solution.

The invention provides a method of inhibiting microorganism growth comprising placing in water susceptible to microorganism growth a device for inhibiting microorganism growth in water, the device comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss, and wherein the device comprises an amount of the moss effective to inhibit microorganism growth in the water. The water can be in a spa, pool, or aquarium. The water can be pumped through the device.

The invention provides a kit comprising sterilized, non-decomposed moss and a device for use in water comprising a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity, wherein the interior cavity can completely enclose the moss. The kit can comprise one or more pH test strips and/or potassium monopersulfate.

The invention provides a method of inhibiting microorganism growth comprising placing in water susceptible to microorganism growth a device for inhibiting microorganism growth in water, the device comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss, wherein the device comprises an amount of the moss effective to inhibit microorganism growth in the water, and periodically shocking the water with an appropriate chemical agent. The chemical agent can be potassium monopersulfate.

The invention provides a method of treating water comprising placing in water a device comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss, and wherein the device comprises an amount of the moss effective to remove cations other than hydrogen ions from the water. The cations can be calcium or iron ions, and substantially all of the calcium or iron ions can be removed from the water. The moss can be compressed and can be in the form of strips. The moss can be sterilized by autoclaving, sterilized by chemical treatment, or sterilized by treatment with ethylene oxide. The moss can be washed with an acidic solution, especially a solution of acetic acid. The moss can be washed with an acidic solution and then washed with a salt solution. The water can be in a spa, pool, or aquarium.

FIGS. 1A to 1C illustrate a suitable device of this invention. FIG. 1A shows device 10 floating in water and FIGS. 1B and 1C shows side and cross sectional views, respectively. Device 10 is adapted to receive a segment of compressed sphagnum moss 15 that has been cut into a desired dimension. The moss is shown in phantom in FIGS. 1A and 1B. A convenient dimension for the moss used in device 10 is about 6×¼×¼ inches (15.2×0.63×0.63 cm). A piece of moss this size weighs about 5 grams. Moss 15 is enclosed in nylon mesh 16, sized to permit the compressed moss to expand. The mesh size is such that it will retain even small particles of moss and prevent it from breaking apart and floating away.

Device 10 comprises a plastic material that is impact resistant, does not dissolve in water, and can be shaped into a desired shape. Device 10 is commercially available as a “floater” from MP Industries of Huntington Beach, Calif. It should be noted that floaters of this type are commonly used with pellets or discs of pool cleaning agents, such as those containing chlorine. Device 10 has been adapted for use with sphagnum moss by adding holes to facilitate passage of water into the device.

Device 10 comprises float portion 20 and flow through portion 30. Float portion 20 is cylindrical, and may be any desired dimension, though typically it is larger in diameter than flow-through portion 30. A useful dimension for the float portion is about 5 inches (12.7 cm) in diameter.

Flow-through portion 30 is a two-part elongated cylinder having core or hollow center 32. First part 33 is attached to floatation portion 20 and is provided with screw threads onto which second part 35 affixes. In this way the length of the flow-through portion can be changed. Second part 35 is fixed in position by means of adjustable collar 34. Second part 35 also has removable cap 37, which is weighted so that device 10 floats in the water as illustrated in FIG. 1.

Slots 38 and holes 39 permit water to flow through the cylinder. The slots and holes may be any desired dimension and can be positioned as desired. A useful length of the flow through portion is about 7 inches (17.8 cm). Cap 37 is removable so that the desired size of the sphagnum moss can be inserted into portion 30. Once exposed to water, the compressed moss expands. The density of expanded moss is such that water can permeate it. Device 10 is sufficient to treat up to about 500 gallons of water (for example, in a whirlpool or spa) for up to 30 days.

FIG. 2A illustrates device 50 floating in water. Device 50 comprises cylindrical portion 60 having core or hollow center 62. Slots 64 and holes 66 permit water to enter the hollow center. Moss 55, shown in phantom in FIG. 2A, is encapsulated by mesh 52, as most clearly shown in FIG. 2B. The moss expands when in contact with the water, filling hollow center 62. Cylindrical portion 60 is shown sealed at one end, with removable cap 57 at the other end. Cap 57 may be weighted so that the maximum length of device 60 stays in contact with the water.

FIG. 3 shows device 70 attached to wall W of a swimming pool, aquarium, hot tub, or the like. Moss 75 is encapsulated by mesh 72 and the mesh is affixed to bracket 77. The mesh is of a sufficient size that particles or fragments of moss will stay within the mesh. The bracket hangs from the wall and the device can remain fixed at this location. Alternatively, device 70 could lie on the bottom of the pool or tub. It could be affixed there or could be held down by a weight. It could also be placed in-line with a filter.

EXAMPLES Example 1

S. papillosum moss, harvested from northern Minnesota, and was prepared for bacterial inhibition testing. The moss species was validated by the University of Minnesota and again upon receipt.

All samples were placed in plastic bags. All raw moss was stored at 4° C. until processed by lab personnel. All pre-dried outside moss samples were stored at room temperature until processed.

The following equipment was used:

-   -   a) Blender, 1.25 L capacity (commercially available as         Osterizer® from Oster)     -   b) Distilled Water (available from Premium Water, Inc.)     -   c) Tissue Sieve, 1 cup capacity (commercially available as         Cellector® E-C Apparatus Corp.)     -   d) 1 L Glass Beaker (commercially available as Pyrex®)     -   e) Sterile Polystyrene Petri Dishes 100×15 mm (commercially         available from Falcon)     -   f) Sterile Polystyrene Petri Dishes 150×15 mm (commercially         available from VWR)     -   g) Autoclave (commercially available from Market Forge)     -   h) Metal Lab Scoop (16.5 cm)/commercially available as Adison         Tissue Forceps from VWR)     -   i) Laminar Flow Hood (commercially available from Baker)

Procedure:

-   -   1) Raw moss was taken out of the bag by hand and picked clean of         any visible, roots, leafs and debris and placed in the blender.         The blender was then filled with moss until it reached         approximately the 1 L mark.     -   2) The blender was then filled with 1 L of distilled water and         shaken manually with the lid on for 30 seconds and drained to         remove any remaining dirt and debris. The process was repeated 2         more times to thoroughly wash the moss.     -   3) The blender was then filled with distilled water again and         the moss was blended using the pulse mode on settings 4 and 5         for 30 seconds each until the moss was homogeneous throughout         the sample.     -   4) The blender was then drained of water. Any remaining water         was then squeezed out by hand from the moss using the tissue         sieve. The squeezed moss was then placed in a clean 1 L beaker.         Steps 1 to 4 were repeated until the 1 L beaker was filled with         processed moss. The beaker was then autoclaved for 20 minutes at         121° C at 15 psi (103.4 MPa) using the liquid setting and         allowed to cool at room temperature.     -   5) Once cooled, the moss was brought to the laminar flow hood         and carefully placed in labeled, pre-weighed Petri dishes using         a sterile lab scoop and forceps. Special care was taken not         contaminate the moss and to pack each dish in a uniform manner.         Once packed, the dishes remain uncovered for at least 72 hours         until the moss was dry. The dried dishes were covered and kept         in the flow hood until used.

Example 2

S. cristatum moss, obtained from Sutton's Moss, Canada, (harvested in New Zealand) was prepared for bacterial inhibition testing. The moss species was validated upon receipt. Handling of the moss samples was identical to that described above in Example 1.

The following equipment was used:

-   -   a) Sterile syringes, individually wrapped 30 cc or 60 cc         (commercially available from Becton Dickenson)     -   b) Sterile syringe filters, 0.45 μm (micrometer) and 0.20 μm         (commercially available as Acrodisc from Pall Gellman)     -   c) Adison tissue forceps (commercially available from VWR)     -   d) 50 cc polypropylene graduated test tubes, sterile pack         (commercially available from Falcon)     -   e) Wax film (Parafilm®, commercially available from American         National Can)     -   f) Laminar flow hood (commercially available from Baker Company)     -   g) Pipetman with sterile graduated polypropylene tips, 25 mL         (commercially available from Becton Dickenson)     -   h) 10 M HCl and 10 M NaOH     -   i) pH Meter (commercially available from Beckman Omega 40)         Reagents and Solutions Preparations: (Depending on liquid used         for treatment)     -   a) Bacto™ Tryptic Soy Broth, 30 g/L (Becton Dickenson)/MEM-Alpha         (Gibco)     -   b) Phosphate Buffered Saline (1×), pH 7.1 (commercially         available from Gibco™)     -   c) HPLC Grade Water (commercially available from J. T. Baker)

Procedure

-   -   a) All liquids used for treatment were either autoclaved or         filter sterilized and stored at a proper temperature prior to         use in this protocol. All treatment steps were done with in the         laminar flow hood using aseptic technique. Tissue forceps used         were autoclaved prior to use.     -   b) After weighing the dried moss, the treatment liquid was         pipetted into the Petri dish at a concentration of one         milliliter of treatment liquid to every 50 mg dried moss. If a         concentration other that 50 mg/mL was used, the process changed         accordingly.     -   c) The Petri dish of moss was wrapped in wax film (Parafilm®)         and refrigerated at 4° C. for one hour.     -   d) The Petri dish was removed from the refrigerator and the moss         was scooped and packed into a 30 cc or 60 cc syringe using         sterile tissue forceps. The plunger of the syringe was         re-inserted and the liquid was squeezed into a sterile 50 mL         polypropylene test tube until all possible liquid was extracted.     -   e) The treatment liquid was filtered through a 0.45 μm syringe         filter, then a 0.2 μm syringe filter and stored at 4° C. until         used.     -   f) Filtered samples were pH adjusted using 1.0 M HCl/NaOH and         sterile filtered with a 0.2 μm syringe filter and stored again         at 4° C. until used in the bacteria inhibition assay.

Example 3

This experiment determined the amount of bacterial growth in Tryptic Soy Broth (TSB) by an inhibition assay.

All S. papillosum and S. cristatum moss treatment samples used in this assay were prepared as described above. TSB was also prepared, autoclaved and stored at 4° C. prior to use.

The following equipment was used:

-   -   a) Beckman® DU-64 Spectrophotometer     -   b) Incubator Oven (commercially available from Boekel         Instruments Model #133000)     -   c) 5 mL and 50 mL Polystyrene Tubes (commercially available from         Falcon)     -   d) 10 L and 1 mL polypropylene tips (commercially available from         Pipetman)

Reagents and Solutions:

-   -   a) Bacto® Tryptic Soy Broth (TSB), 30 g/L (commercially         available from Becton Dickenson)     -   b) Escherichia Coli frozen culture stock grown in TSB for a         minimum of 3 log growth phases (Clinical isolate)     -   c) Staphylococcus Aureus frozen culture stock grown in TSB for a         minimum of 3 log growth phases. (ATCC Strain #29213 (American         Type Culture Collection of Manassas, Va.))     -   d) Distilled Water (commercially available from Premium Water         Inc.)     -   e) TSB treatment sample of S. papillosum moss and New Zealand         moss

Procedure:

-   -   1) TSB nutrient broth was prepared by adding 30 g/L Bacto®         Tryptic Soy Broth to distilled water. The solution was stirred         with a stir-bar until all the powder was dissolved and         autoclaved at 121° C. for 20 minutes. The S. papillosum sample         was prepared as described in B, above. One mL of the solutions,         TSB or moss-treated TSB sample, was pipetted into 3 to 5 mL         polystyrene test tubes.     -   2) Frozen aliquots of E. coli and S. aureus stored at −20° C.         were allowed to thaw to room temperature. Once thawed, 100 μL of         each bacterial stock was added to a 10 mL aliquot of TSB. Each         tube was then capped, thoroughly mixed, labeled and placed in         the incubator at 37° C.     -   3) Ten 1 L of bacteria stock was pipetted into the one mL         solutions and the tubes were incubated at 37° C. for the desired         time. One tube in each sample and time point did not receive         bacteria in order to serve as the blank.     -   4) The solutions were removed from the 37° C. oven at the         assigned time points and placed in an ice bath. Samples were         then immediately read on the spectrophotometer at 550 nm. The         absolute OD value was sample minus the blank. Inhibition was         measured as percent decrease in OD value vs. the appropriate TSB         control sample.

Example 4

The following data illustrate the effect of treatment of bacterial growth media (i.e., Tryptic Soy Broth) with various moss species according to the procedure in Example 3. Non-sphagnum species are very poor at preventing E. coli growth. Of the moss tested below, the most effective sphagnum mosses to prevent E. coli growth were S. papillosum and S. cristatum. “N” refers to the number of tests, “Range” presents the highest and lowest numbers obtained for these tests; and “Mean” refers to the mean value of the tests.

% Inhibition of Bacterial Growth Mean N Range Sphagnum Species S. papillosum (MN) 48 10 26-71 S. cristatum (NZ - Sutton Moss) 45 8 31-62 S. magellanicum (WI - Mosser Lee) 34 7 21-43 S. fuscum (MN) 20 1 — S. falcatulum (NZ) 7 2  2-11 Non- Sphagnum Species Sheet Moss (WI - Mosser Lee) 4 1 — Spanish Moss (WI - Mosser Lee) −2 1 —

Example 5

TSB was treated with S. papillosum and the ability of this solution to support bacterial growth was measured according to Example 3. The percent inhibition of bacterial growth for E. coli (clinical isolate) and S. aureus (ATCC Strain # 29213) is reported. A TSB Control sample and moss-treated TSB solutions (MT-TSB) are reported below. The OD of a blank (B) is subtracted from the measured OD (Meas.) of the sample to obtain the reported Value.

Test Material E. coli S. aureus B Meas. Value B Meas. Value TSB 0.063 0.744 0.681 0.063 0.250 0.187 (Control) 0.726 0.663 0.257 0.194 Mean 0.672 0.191 SD 0.013 0.005 MT-TSB 0.109 0.662 0.553 0.109 0.279 0.170 (5 mg/mL) 0.714 0.605 0.285 0.176 Mean 0.579 0.173 SD 0.037 0.004 % Inhibition 13.84 9.19 MT-TSB 0.131 0.575 0.444 0.131 0.278 0.147 (10 mg/mL) 0.748 0.617 0.274 0.143 Mean 0.531 0.145 SD 0.122 0.003 % Inhibition 21.06 23.88 MT-TSB 0.173 0.662 0.489 0.173 0.276 0.101 (25 mg/mL) 0.652 0.479 0.284 0.111 Mean 0.484 0.107 SD 0.007 0.006 % Inhibition 27.98 43.83 MT-TSB 0.243 0.599 0.356 0.243 0.355 0.112 (50 mg/mL) 0.564 0.321 0.352 0.109 Mean 0.339 0.111 SD 0.025 0.002 % Inhibition 49.63 41.99 MT-TSB 0.284 0.388 0.104 0.284 0.361 0.077 (75 mg/Ml) 0.430 0.146 0.355 0.071 Mean 0.125 0.074 SD 0.030 0.004 % Inhibition 81.40 61.15 MT-TSB 0.274 0.322 0.048 0.274 0.322 0.048 (100 mg/mL) 0.339 0.065 0.310 0.036 Mean 0.057 0.042 SD 0.012 0.008 % Inhibition 91.59 77.95

Example 6

This example demonstrates that treatment with moss does not kill the bacteria but it does inhibit their growth. A fluorescence assay, commercially available from Molecular Probes, Eugene, Oreg., Kit No. L-7012, was used to determine the viability of bacteria. This system uses mixtures of green and red fluorescent nucleic acid stains that have differing ability to penetrate viable and non-viable bacterial cells. The green fluorescent strain, which emits at 500 nm, binds to both viable and non-viable bacteria. The red fluorescent strain, which emits at 650 nm, binds only to non-viable bacteria. Therefore, a bacterial sample containing a higher proportion of non-viable bacteria will have an altered staining ratio. The data show that for both E. coli and S. aureus, the ratio of viable to non-viable bacteria remains the same as in the control sample.

Procedure:

-   -   1. 100 μL was incubated in 10 mL of media (pH controlled TSB         and S. papillosum sample, as prepared in Examples 1 and 2,         respectively) for 3 hours at 37° C.     -   2. This mixture was centrifuged to concentrate the bacteria,         which was then resuspended in 10 mL phosphate buffered saline         (PBS).     -   3. Three mL of resuspended bacteria were added to each of three         cuvettes.     -   4. 40 μL Styo-9 dye was mixed with 40 μL Propidium Iodide dye.         Caution should be used as these compounds are believed to be         carcinogens.     -   5. 9 μL of the mixed dye solution was added to each cuvette and         stored in the dark for 15 minutes.     -   6. Two PBS cuvettes were prepared with no dye and two PBS         cuvettes were prepared with dye to be used as blanks.     -   7. The solutions were mixed thoroughly. The fluorescence         intensity is measured at 500 nm (with absorption at 480 nm) and         at 650 nm (with absorption at 490 nm). The ratio of these two         values relates to the degree of viability of the bacterial         culture.         The following tables report the fluorescence intensity at two         wavelengths for bacterial samples in two different media. The         intensity of fluorescence at 500 nm over the intensity of the         fluorescence at 650 nm creates a ratio which relates to the         degree of viability of the bacterial culture. The mean of three         TSB and three moss-treated TSB samples (MT-TSB) is reported         below. In each case, the percent of inhibition is compared to a         control sample.

Viability Assay for E. coli (clinical isolate) Media 500 nm 650 nm Ratio 500/650 TSB 505.117 5.783 87.3228 MT-TSB of 130.1833 1.5167 85.8352 S. papillosum

Viability Assay for S. aureus (ATCC Strain #29213) Media 500 nm 650 nm Ratio 500/650 TSB 80.117 3.533 22.6745 MT-TSB of 45.055 2.0667 21.7984 S. papillosum The data show that there is no significant change in the ratios between TSB and the moss-treated TSB, indicating that the effect of the moss is bacteriostatic rather than bactericidal.

Example 7

Various bacteria were treated with S. papillosum TSB (concentration of 50 mg/mL) according to Example 3. The percent inhibition of bacterial growth is reported. Both a TSB Control sample and moss-treated TSB solutions (MT-TSB) are reported below. The “Value” is obtained by subtracting the optical density (OD) of a blank (B) from the measured OD (Meas.) of a sample.

Two studies were done and are denoted (1) and (2) below.

Test Material (1) E. coli S. aureus (clinical isolate) ATCC # 29213 B Meas. Value B Meas. Value TSB 0.034 0.694 0.660 0.034 0.273 0.239 (Control) 0.718 0.684 0.257 0.253 Mean 0.672 0.246 SD 0.017 0.010 MT-TSB 0.219 0.542 0.323 0.219 0.362 0.143 0.572 0.353 0376 0.157 Mean 0.338 0.150 SD 0.021 0.010 % Inhibition 49.7 39.02

Test Material (2) E. coli S. aureus B Meas. Value B Meas. Value TSB 0.043 0.693 0.650 0.043 0.332 0.289 (Control) 0.667 0.624 0.327 0.284 Mean 0.637 0.287 SD 0.018 0.004 MT-TSB 0.247 0.492 0.245 0.247 0.394 0.147 0.498 0.251 0.428 0.181 Mean 0.248 0.164 SD 0.004 0.024 % Inhibition 61.07 42.76

Test Material (1) S. epidermidis P. aeruginosa ATTC # 12228 ATTC # 10145 B Meas. Value B Meas. Value TSB 0.034 0.388 0.354 0.034 0.175 0.141 (Control) 0.412 0.375 0.167 0.133 Mean 0.366 0.137 SD 0.017 0.006 MT-TSB 0.219 0.542 0.323 0.219 0.321 0.102 0.572 0.353 0.331 0.112 Mean 0.338 0.107 SD 0.021 0.007 % Inhibition 53.26 21.90

Test Material (2) S. epidermidis P. aeruginosa B Meas. Value B Meas. Value TSB 0.043 0.349 0.306 0.043 0.204 0.161 (Control) 0.327 0.284 0.186 0.143 Mean 0.295 0.152 SD 0.016 0.013 MT-TSB 0.247 0.428 0.181 0.247 0.371 0.124 0.444 0.197 0.340 0.093 Mean 0.189 0.109 SD 0.011 0.022 % Inhibition 35.93 28.62

Test Material (1) C. albicans A. amsterodami ATTC # 10231 ATTC # 1001 B Meas. Value B Meas. Value TSB 0.034 0.068 0.034 0.034 0.053 0.019 (Control) 0.069 0.035 0.047 0.013 Mean 0.035 0.016 SD 0.001 0.004 MT-TSB 0.219 0.249 0.030 0.219 0.231 0.012 0.245 0.026 0.229 0.010 Mean 0.028 0.011 SD 0.003 0.001 % Inhibition 18.84 31.25

Test Material (2) C. albicans A. amsterodami B Meas. Value B Meas. Value TSB 0.043 0.1019 0.058 0.043 0.067 0.024 (Control) 0.057 0.044 0.071 0.028 Mean 0.051 0.026 SD 0.010 0.003 MT-TSB 0.247 0.275 0.028 0.247 0.268 0.021 0.292 0.045 0.254 0.007 Mean 0.037 0.014 SD 0.012 0.010 % Inhibition 28.43 46.15

Example 8 Effect of Acid Treatment of the Moss

Compressed sticks of S. cristatum moss (obtained from Sutton's Moss, Canada (harvested in New Zealand)) were soaked in four increasing concentrations of Fe (Fe standard in concentrated HCl, 0, 0.5, 5, 50 mg/L, available from Ricca Chemicals, Arlington, Tex.) at 50 mg moss/ml in distilled water. The soaked moss was stored overnight at 4 C. The Fe solutions were extracted by syringe, filtered and measured for Fe by inductively coupled plasma atomic emission spectrometry analysis. The results showed that the moss bound significant amounts of Fe, up to 15 mg/L in the 50 mg/L sample. This experiment was run with distilled water washed moss resulting in similar results. However, it was noted that the Fe spiked samples had a low pH. Since optimal binding is at pH 4 to 6, we adjusted the pH up to between 4 and 7 on the next experiment. When the pH of the Fe samples was brought up, the Fe started to precipitate. The moss removed all of the Fe from the sample (up to 25 mg/L). It was then decided that ions bound to the moss before use could affect the cation binding tests and methods to remove the cations from the moss should be investigated.

When developing the method for acid washing Sphagnum moss (not peat moss, which is decomposed moss), two different acids were first used. One batch of moss (approx. 5 g) was constantly stirred in 3.5 L of distilled water pH adjusted to 1 with concentrated HNO₃. For the other batch of moss, a 2% solution of glacial acetic acid was used. The washes were stirred for 1 hour, then the supernatant was filtered off and new wash solution was put on the moss. This was repeated for a total of four acid washes. The acid washes were followed by 4 distilled water washes carried out the same way. At the end of the distilled water washes, the conductivity was similar to that of distilled water. The two acids removed similar amounts of ions; therefore acetic acid was routinely used for washing the moss thereafter.

It was decided that a metal that was soluble at neutral pH would be better suited to test binding capacity and test for improvement of binding with acid washed Sphagnum moss vs. non-washed moss. Calcium was chosen for this purpose. The moss used was the S. cristatum moss described earlier in this example, the acid used was a 2% solution of glacial acetic acid, and the wash was performed as described in the preceding paragraph. The first test showed the opposite of what was expected, the non-washed moss bound the most and the acid washed moss bound the least. When the pH of the samples was checked, it was discovered that the binding ability correlated with pH. The acid washed moss reduced the pH of the solutions, which affected the ion binding. To eliminate this problem, acid washed moss was washed with a high salt solution to displace the H⁺ ions with Na. The high salt solution was 1M sodium acetate and approximately 5 g of moss was constantly stirred in 3.5 L of this sodium acetate solution for one hour, and then the wash was repeated. These two sodium acetate washes were followed by four washes with distilled water, each wash for one hour, and each was carried out the same way. The acid/salt-washed moss was tested; the pH of the extract did not drop and showed a significant improvement of binding over distilled water and non-washed moss as can be seen in the following table (concentrations of Ca are in ppm).

Starting Resulting Moss treatment [Ca] Average [Ca] Stdev pH Control 0 −1.08 0.61 6.02 Acetic Acid, Acetate 0 −0.97 0.45 7.62 Washed No wash 0 −0.14 0.51 5.26 Distilled water washed 0 0.36 1.32 5.13 Acetic Acid, Acetate 100 −1.40 0.25 6.62 washed No wash 100 11.24 0.00 4.81 Distilled water washed 100 16.89 1.17 4.54 Control 100 88.76 0.05 6.65 Acetic Acid, Acetate 200 −0.33 0.87 6.17 washed No wash 200 46.47 5.88 4.82 Distilled water washed 200 53.55 4.42 4.61 Control 200 198.10 1.83 6.76 The pH of the extracts varied by up to 2 pH units, so it was still difficult to distinguish between the effects of acid washing and pH. Therefore a new method to test for binding of the moss was developed that would allow adjustment of pH while the moss was still in the sample solutions. This was accomplished by using multi-well plates, small stir bars and 10 mg/ml moss concentrations. After the solutions were on the moss for approximately one-half hour, the pH's of the solutions were all adjusted to within 0.25 pH units of 6.5. This allowed for the testing of acid/salt washed moss and acid only washed moss. The results are shown below. The averages shown are the averages of two samples.

Starting Resulting Moss treatment [Ca] Average [Ca] Stdev Acetic Acid/Na acetate 0.00 6.93 0.72 washed Acetic Acid washed 0.00 6.16 0.16 Distilled water washed 0.00 6.85 0.31 No wash 0.00 8.54 1.56 Control 0.00 8.10 0.31 Acetic Acid/Na acetate 100.00 6.78 0.31 washed Acetic Acid washed 100.00 6.82 0.26 Distilled water washed 100.00 20.73 1.09 No wash 100.00 26.25 0.72 Control 100.00 92.27 1.56 Acetic Acid/Na acetate 500.00 307.28 7.25 washed Acetic Acid washed 500.00 319.25 8.13 Distilled water washed 500.00 375.18 3.36 No wash 500.00 382.85 4.38 Control 500.00 454.30 8.91 With the pH's adjusted to be within 0.5 pH units of each other; the pH effect is eliminated and the significantly improved binding capacity of the acid washed mosses can be seen. The acid/salt washed moss bound slightly better than the acid only washed moss and the distilled washed slightly better than the non-washed moss, but barely enough to be significant.

Thus, the moss was shown to bind both Fe and Ca ions, and therefore is effective in water treatment because the removal of one or both of these ions is a goal of water treatment.

The above description and the drawings are provided for the purpose of describing embodiments of the invention and are not intended to limit the scope of the invention in any way. It will be apparent to those skilled in the art that various modifications and variations can be made without departing from the spirit or scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents. 

1. A device for use in water comprising: (i) a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity; and (ii) a moss contained within the interior cavity, wherein the carrier completely encloses the moss.
 2. The device of claim 1, wherein the carrier comprises a float.
 3. The device of claim 1, wherein the moss is enclosed within a mesh bag.
 4. The device of claim 1, wherein the carrier comprises one or more weights.
 5. The device of claim 1, wherein the moss is non-decomposed moss.
 6. The device of claim 5, wherein the moss is sphagnum moss.
 7. The device of claim 5, wherein the moss is selected from the group consisting of sphagnum papillosum, sphagnum cristatum, and mixtures thereof.
 8. The device of claim 7, wherein the moss is sphagnum papillosum.
 9. The device of claim 7, wherein the moss is sphagnum cristatum.
 10. The device of claim 7, wherein the moss comprises sphagnum papillosum only.
 11. The device of claim 7, wherein the moss comprises sphagnum cristatum only.
 12. The device of claim 7, wherein the moss comprises a mixture of sphagnum papillosum and sphagnum cristatum only.
 13. The device of claim 5, wherein the moss is compressed.
 14. The device of claim 13, wherein the moss is in the form of strips.
 15. The device of claim 5, wherein the moss has been sterilized.
 16. The device of claim 5, wherein the moss has been washed with an acidic solution.
 17. The device of claim 5, wherein the moss has been washed with a solution of acetic acid.
 18. The device of claim 5, wherein the moss has been washed with an acidic solution and then washed with a salt solution.
 19. A kit comprising sterilized, non-decomposed moss and a device for use in water comprising a carrier having an interior cavity and one or more openings allowing ingress to and egress from the interior cavity, wherein the interior cavity can completely enclose the moss.
 20. The kit of claim 19, wherein the carrier comprises a float.
 21. The kit of claim 19, wherein the carrier comprises one or more weights.
 22. The kit of claim 19, wherein the moss is enclosed within a mesh bag.
 23. The kit of claim 19, wherein the moss is sphagnum moss.
 24. The kit of claim 19, wherein the moss is compressed.
 25. The kit of claim 19, wherein the moss has been sterilized.
 26. The kit of claim 19, wherein the moss has been washed with an acidic solution. 